Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH. Issue 8 (13th June 2018)

• Record Type: Journal Article
• Authors: Shariati, Gholamreza; Saberi, Alihossein; Hamid, Mohammad; Galehdari, Hamid; Sedaghat, Alireza; Abdorasuli, Nehzat
• Is Part Of: Clinical case reports. Volume 6:Issue 8(2018)
• Page Start: 1464
• Page End: 1469
• Publication Date: 2018-06-13
• Subjects: 1q22‐q25.1 -- cleft lip/palate -- oligo array CGH -- small hands and feet; Medicine -- Periodicals; 616.09
• DOI: 10.1002/ccr3.1604
• Languages: English
• ISSNs: 2050-0904

Abstract

Key Clinical Message: We present prenatal diagnosis of a case with a rare de novo interstitial deletion of 1q21‐q25.1 by oligo array CGH and provide detailed information on unbalanced gene content and the breakpoints. The affected fetus was delivered at 37 weeks' gestation with a unique clinical phenotype. Abstract : We present prenatal diagnosis of a case with a rare de novo interstitial deletion of 1q21‐q25.1 by oligo array CGH and provide detailed information on unbalanced gene content and the breakpoints. The affected fetus was delivered at 37 weeks' gestation with a unique clinical phenotype.